Multilayer cling film

ABSTRACT

A film comprising a release layer and an adhesive layer, wherein the thickness of the film is less than 25 microns.

In the plastic film area a very well known type of film is the so called “cling film” or “kitchen wrap”. This film is used by the layman in order to protect ready food from spoilage in everyday kitchen use. Well known films of this type are the Saranex® film in the US and similar films in Europe, Australia and Japan.

This kind of films in order to perform must combine a certain range of properties.

-   -   1. The films must have enough adhesiveness in order to cling to         plastic kitchen bowls (e.g. Tupperware® type) so that the food         stored is protected.     -   2. They must have enough elongation to be effectively used in         practical everyday applications.     -   3. They must be able to unwind easily during everyday use in the         kitchen (films are used in reel form wound around a paper or         plastic core).     -   4. They must be able to be torn efficiently.     -   5. They must be environmentally friendly and as thin as         practically possible

In the today state of the art, two basic films are used for this application. First one is based on LLDPE (linear low density polyethylene) while the second is based on PVDC (polyvinylidene chloride). Both have certain advantages and disadvantages.

LLDPE films are economical to manufacture, have enough cling properties and are environmentally friendly. But on the other hand, they do not have odour barrier properties and they are notoriously known for being difficult to cut and difficult to unwind. This type of film is the most common in Europe.

PVDC films are very difficult to produce and are expensive and considered as non environmentally friendly(due to chlorine presence in PVDC). They have excellent odour barrier and acceptable cling properties.

Sometimes, instead of PVDC a PVC film is used. This solution is not considered viable in many markets due to the phthalate plasticizers used in the production process of soft PVC. In general, the plasticizer migration from the film to the foods and the chlorine content of PVC create a non-environmental friendly image of the material.

In general all the above films suffer from difficult unwinding due to stickiness of both sides of the film. This effect is annoying to the everyday users of the films e.g. housewives. This deficiency is remedied by the present invention.

The present invention provides film having a thickness of less than 25 microns. The film comprises at least two layers namely a release layer and an adhesive layer and is able to remedy the deficiencies of the films of the current state of the art. Further the present invention relates to the use of said film as a kitchen wrap film and further to the use of said film for wrapping food.

In the prior art literature there have been attempts to develop a cling film with release properties.

For example, U.S. Pat. No. 8,197,927 describes a film where the release layer is a blend of polypropylene and high density polyethylene. The patent teaches that coefficient of friction properties are improved after stretching. Nevertheless, the coefficient of friction values are in the range of 0.49 which is quite high.

EP 2 582 519 describes also a release layer. But according to the teachings of this application the slip and antiblock masterbatches if present must not hinder the cling properties of the release layer to the adhesive cling layer. This means that the coefficient of friction in practice will be still high and the film will be somewhat difficult to unwind.

The present invention provides a film comprising at least two layers one of which is an adhesive layer and the other is a release layer, where the kinetic coefficient of friction of the release layer measured according to ASTM D 1894 (film to film measurement) is less than 0.4, preferable less than 0.3, more preferably less than 0.25 and even more preferably less than 0.2.

FILM OF THE INVENTION

The film of the present invention has a thickness of less than 25 microns, preferably less than 20 microns, more preferably less than 18 microns, even more preferably less than 17 microns, and even more preferably less than 15 microns.

The film of the invention has preferably the following structure:

Release Layer/adhesive Layer

Release Layer/tie Layer/adhesive Layer

Release Layer/abuse/tie Layer/adhesive Layer

Release Layer/tie Layer/abuse Layer/tie Layer/Adhesive Layer

Or any other structure that comprises the above basic structures.

In a most preferable version of the film the adhesive layer is the layer used as inner layer (=the film surface that is closest to the packed food).

Definitions:

In this application the following definitions are used:

The term “film” refers to a flat or tubular flexible structure of thermoplastic material.

The term “heat shrinkable” refers to a film that shrinks at least 10% in at least one of the longitudinal and transverse directions when heated at 90° C. for 4 seconds. The shrinkability is measured in water according to ASTM 2732. For temperatures like 100 ° C. or more, glycerine is used as a reference liquid.

The term “total heat shrinkability” refers to the sum of heat shrinkability at the MD direction and heat shrinkability at the TD direction. In all cases, ASTM 2732 is used for measurement of shrinkabilities.

The term “multilayer” refers to a film comprising 2 or more layers.

The phrase “longitudinal direction” or “machine direction” herein abbreviated “MD” refers to a direction along the length of the film.

The phrase “outer layer” refers to the film layer which comes in immediate contact with the outside environment (atmosphere). The outer layer in the present invention is a “release layer”, i.e. a low- or non-adhesive antistick layer.

The phrase “inner layer” refers to the film layer that comes in direct contact with the product packed.

As used herein, the term “homopolymer” refers to a polymer resulting from polymerization of a single monomer.

As used herein, the term “copolymer” refers to a polymer resulting from polymerization of at least two different polymers.

As used herein, the term “polymer” includes both above types.

As used herein, the term “polyolefin” refers to any polymerized olefin, which can be linear, branched, cyclic, aliphatic, substituted or unsubstituted. More specifically, included in the term polyolefin are homopolymers of olefin, copolymers of olefin, copolymers of an olefin and a non olefinic comonomer (such as ester) etc.

Specific examples include polyethylene homopolymer, polypropylene homopolymer, polybutene homopolymer, ethylene alpha olefin copolymer, propylene alpha olefin copolymer, butene alpha olefin copolymer, ionomer, ethylene ester copolymer etc.

As used herein the term “polyethylene” identifies polymers consisting essentially of the ethylene repeating unit. The ones that have a density more than 0.940 are called high density polyethylene (HDPE), the ones that are have less than 0.940 are low density polyethylene (LDPE).

As used herein the phrase “ethylene alpha olefin copolymer” refers to polymers like linear low density polyethylene (LLDPE), medium density polyethylene (MDPE), very low density polyethylene (VLDPE), ultra-low density polyethylene (ULDPE), metallocene catalysed polymers and polyethylene plastomers and elastomers.

As used herein the term “homogeneous ethylene alpha olefin copolymers” refer to ethylene alpha olefin copolymers having a molecular weight distribution less than 2.7 as measured by GPC. Typical examples of these polymers are AFFINITY® from DOW or Exact® from Exxon.

As used herein the phrase “styrene polymers” refers to styrene homopolymers such as polystyrene and to styrene copolymers such as styrene-butadiene copolymers, styrene-butadiene-styrene copolymers, styrene-isoprene-styrene copolymers, styrene-ethylene-butadiene-styrene copolymers, ethylene-styrene copolymers and the like.

As used herein the phrase “ethylene methacrylate copolymers” refers to copolymers of ethylene and methacrylate monomer. The monomer content is less than 40% per mol.

As used herein the phrase “ethylene vinyl acetate copolymer” or EVA refers to copolymers of ethylene and vinyl acetate.

As used herein the phrase “ethylene ester copolymer” includes any polymer made from ethylene and ester monomers. It is obvious that this term includes EVAs, EMAs and other polymers.

As used herein the term “oxygen barrier polymer” refers to polymers which have the property to limit the passage of oxygen through a film or a layer comprising the polymer. Common materials are EVOH, PVDC or polyamide.

As used herein, the term EVOH refers to saponified products of ethylene vinyl ester copolymers. The ethylene content is typically in the range of 25 to 50% per mol. All the later references to EVOH ethylene content will be in % per mol.

As used herein the term PVDC refers to a vinylidene chloride copolymer wherein a major amount of the copolymer comprises vinylidene chloride and a minor amount of the copolymer comprises one or more monomers such as vinyl chloride and/or alkyl acrylates and methacrylates.

As used herein the term “polyamide” refers to homopolymers and copolymers. Polyamide 6, polyamide 66, polyamide 12, polyamide 6/66, polyamide 6/12, polyamide elastomers, MXD polyamides and other copolymers are specifically useful for the invention.

As used herein the term “polyester” refers to polymers comprising terephthalate units. Examples of polyesters are PET (polyethylene terephthalate), PBT (polybutylene terephthalate), polyester elastomer (block copolymer comprising ester or ether units), PTT and other similar polymers.

As used herein, the term “ionomer” comprises the copolymers of ethylene and methacrylic or acrylic acid being metal neutralized. An example of such material is Surlyn® from Dupont.

As used herein, the term “polypropylene” refers to polymers incorporating propylene structural units. Examples of these, are homo polypropylenes, random copolymers of propylene and ethylene, block copolymers of propylene and ethylene, copolymers or blends of propylene and rubber (such as blends of polypropylene and ethylene propylene rubber), propylene ethylene alpha olefin terpolymers and others.

These polymers may be isotactic, syndiotactic or atactic. Isotactic configuration is preferred.

As used herein the term “self adhesive material” refers to materials that when produced into film form can be bonded to themselves by pressure only without the need to be heated. The bonding level which separates self adhesive from non self adhesive materials is 5 g/15 mm when the bonding has been done on a 100×1500 mm film piece with a pressure of 3 bar at a temperature of 23 ° C. and 50% relative humidity and with a contact time of 5 seconds. Values of more than 5 g/15 mm according to this test show that the material is self adhesive whereas values of lower than 5 g/15 mm show the film being non self adhesive.

As used herein the term “substantially non resilient material” refers to materials or material compounds comprising at least 40% per weight inorganics like calcium carbonate, titanium dioxide, wollastonite, mica, glass fibers, dolomite and the like. The rest percentage per weight can be polyethylene, polypropylene, styrene polymer or other thermoplastic material.

As used herein the term “tackifier” refers to low molecular weight materials used to increase the stickiness of the surface of an adhesive. Typical examples are rosins and their derivatives, terpenes and modified terpenes, hydrogenated hydrocarbon resins, C5 aliptatic resins, C9 aromatic resins, C5/C9 resins, terpene/phenol resins and the like.

All measurement methods mentioned herein are readily available for the skilled person. For example, they can be obtained from the American National Standards Institute at: www.webstore.ansi.org

All percentages are based on weight per weight ratio, except when otherwise stated.

The grs/square meter is same as g/m². Both are expressing the weight to surface ratio.

DETAILED DESCRIPTION OF LAYERS

Inner Layer (Adhesive)

The inner layer comprises an adhesive material.

In a further preferred embodiment, the weight of the inner layer is less than 6 g/m², more preferably less than 5 g/m².

In a preferred version, the adhesive material comprises ethylene vinyl acetate copolymer where the vinyl acetate weight ratio is at least 20%, more preferably at least 25%, even more preferably at least 25%, even more preferably at least 40%.

In another preferred version the adhesive material is a propylene ethylene copolymer where the ethylene content is at least 10% per weight.

In another preferred version the adhesive material comprises an ethylene alpha olefin copolymer with density less than 0.9 g/cm³, even more preferably less than 0.880 g/m³. Preferred alpha olefins are butene, hexene or octene.

In another preferred version, the adhesive material comprises a maleic anhydrite grafted polyolefin. Examples are maleic anhydrite grafted ethylene vinyl acetate copolymer of linear low density polyethylene.

In another preferred version, the adhesive material comprises styrene copolymers with styrene content less than 50% per weight. Typical examples are styrene butadiene styrene copolymers, styrene isoprene styrene copolymers, styrene ethylene butadiene copolymers and the like.

In another preferred version, the adhesive material comprises ethylene methyl acrylate copolymer with a methyl acrylate content of at least 20%.

In another preferred version, the adhesive material comprises ethylene butyl acrylate material with a butyl acrylate content of at least 15%.

In another preferred version, the adhesive material comprises poly-isobutylene polymer (PIB) or polybutene copolymer.

The inner layer may comprise also non self adhesive materials such as polyolefins (preferably polyethylene homopolymers or copolymers) but not to the extent that the adhesive properties are compromised.

In another version, the inner layer may comprise tackifiers such as hydrocarbon resins, terpene resins, rosins and the like. Typical examples are Escorez® materials from Exxon.

In a further preferred version the inner layer may comprise materials such as “substantially non resilient materials” (SNR). See the above definition of this term.

In a preferred version of the invention, the adhesive material in the inner layer is an extrudable material, meaning that it is melt processed by extrusion process.

Outer Layer (Release Layer)

As defined above, the phrase “outer layer” refers to the film layer that comes in direct contact with the environment.

Preferred materials for the outer layer include polyolefins, such as low density polyethylene, high density polyethylene, ethylene ester copolymer, ethylene alpha olefin copolymer and polypropylene. Ionomers and styrene copolymers are also possible. Ethylene alpha olefin copolymer is particularly preferred.

According to a further embodiment, the present invention is of the same configuration where outer layer comprises a “substantially non resilient material” (SNR).

In a preferred version of the invention, the SNR material is at least 10 percent, preferably at least 20, preferably at least 30 percent per weight of the outer layer.

In a preferred version the outer layer comprises at least one release agent that is a polymer or chemical substance that allows the surface tension of the outer side to decrease. The reason for this is to allow the easy unwinding of the reel when the inner and the outer side come in contact one to the other. Preferred release agents are organic lubricants (such as erucamide or oleamide) and silicone or siloxane based lubricants.

In a preferred version the release layer comprises at least 200 ppm of an amide based lubricant. Typical amide based lubricants are erucamide, oleamide, stearamide, oleyl palmitamide, behenamide and the like. In a more preferred version, the release layer comprises at least 500 ppm of an amide based lubricant as of above.

In a further preferred version, the film comprises a PDMS based lubricant in a percentage from 0.1 to 10%, preferably.

Tie Layers

In the tie layers typical adhesive resins like maleic anhydride modified polyolefins may be used. Typical examples are BYNEL® from Dupont and OREVAC® from Arkema.

In another preferred version the tie layers comprise low density polyethylene, linear low density polyethylene, ethylene ester copolymers such as EVA, EMA or EBA and other polyolefin homopolymers, copolymers and terpolymers.

In another preferred version of the invention, polyamide could be used as tie layer. In that case a tie layer is needed between polyamide and polyolefins.

Abuse Layers

In the abuse layers the use of polyolefin homopolymers and/or copolymers is preferred. Polyamide, polystyrene and polyester is also possible.

General

The preferred production method for the film is the hot blown film method, which is well known in the art. Other methods like extrusion through flat cast die are also possible.

Additives well known in the art may be used in one or more layers of the present invention. Slip additives, antiblock additives, antifog, polymer processing aids may be used if pertinent.

In order to increase the mechanical properties the film may be crosslinked with one of the following methods: E-beam radiation, gamma radiation, moisture crosslinking using silane grafting compounds, peroxide crosslinking.

The film may be in tubular form or sealed at the edges or single sheet configuration. Centerfold configuration is also possible.

Without further elaboration, it is believed that one skilled in the art can, using the preceding description, utilize the present invention to its fullest extent. The preceding preferred specific embodiments are, therefore, to be construed as merely illustrative, and not limitative of the remainder of the disclosure in any way whatsoever.

In the foregoing and in the examples, all temperatures are set forth uncorrected in degrees Celsius and, all parts and percentages are by weight, unless otherwise indicated.

The entire disclosures of all applications, patents and publications, cited herein and of corresponding European application No. 17197778.8, filed Oct. 23, 2017, are incorporated by reference herein.

EXAMPLES Example 1

A 5 layer film is produced in a commercial hot blown film line with the following recipe:

Outer layer 75% EAO1 + 15% SNR1 + 10% slip antiblock masterbatch Tie layer EAO1 Abuse layer EAO1 Tie layer EAO1 Inner layer Ethylene vinyl acetate copolymer comprising 80% vinyl acetate per weight (= a blend of EVA with 90% vinyl acetate + 10% low density polyethylene)

See table 1

The thickness (in microns) of the structure is 5/1.5/1.5/1.5/3 starting from the inner and going to the outer layer.

TABLE 1 Density Type Description g/cm³ EAO1 Ethylene octene copolymer (LLDPE) 0.92 SNR1 Calcium carbonate compound 1.6

The slip antiblock masterbatch comprises 5% of erucamide, 10% silica and the balance LDPE.

Example 2

A 5 layer film is produced in a commercial hot blown film line with the following recipe:

Outer layer 75% EAO1 + 15% SNR1 + 8% slip antiblock masterbatch + 2% PDMS masterbatch Tie layer EAO1 Abuse layer EAO1 Tie layer EAO1 Inner layer A blend of 90% ethylene vinyl acetate copolymer comprising 80% vinyl acetate per weight + 10% calcium carbonate polyethylene compound

The thickness of the structure (in microns) is 4/1.5/1.3/1.5/3

Testing the Material as Kitchen Wrap

The films coefficient of friction was measured as per ASTM D 1894 using a THWING-ALBERT® coefficient of friction tester in film to film measurement. Therefore, according to the teachings of the ASTM D1894 the cof of the outer (release side) was tested in a film to film measurement.

Therefore, for film 1 outer release side a coefficient of friction of 0.19 was measured and for film 2 a value of 0.24 was measured.

The values represent the kinetic coefficient of friction. Static coefficient of friction was slightly higher (as expected to the person skilled in the art) in the range of 0.25-0.35.

For the commercial PVC film a coefficient of friction of 0.9 was measured. The side was sticky therefore the measurement was difficult to do.

Then all three films were evaluated as per “easy to unfold” feature. Films 1 and 2 were much easier to unfold and unwind versus the commercial PVC film. Therefore the practical applicability of the invention is justified.

The preceding examples can be repeated with similar success by substituting the generically or specifically described reactants and/or operating conditions of this invention for those used in the preceding examples.

From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention and, without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions. 

1. A film with thickness of less than 25 microns comprising a release layer and an inner adhesive layer, wherein the kinetic coefficient of friction of the release layer surface of the film measured according to ASTM D 1894 (film to film measurement) is less than 0.4.
 2. The film of claim 1, wherein the release layer comprises at least 200 ppm of an amide lubrican.
 3. The film of claim 1, wherein the film thickness is less than 20 microns.
 4. The film of claim 1, wherein the film thickness is less than 17 microns.
 5. The film of claim 1, wherein the release layer of the film comprises from 0.1 to 10% by weight PDMS.
 6. The film of claim 1, wherein the adhesive layer comprises ethylene vinyl acetate copolymer.
 7. The film of claim 1, wherein the release layer comprises polyolefin homopolymer or copolymer.
 8. The film of claim 1, wherein between the adhesive and release layer there is a least one tie layer.
 9. The film according to claim 1, wherein the film comprises a kitchen wrap film.
 10. (canceled)
 11. A method for wrapping food using the film of claim
 1. 